Our buddy Mike lost his battle with ALS March 27, 2018 but his fighting spirit lives on through his friends and loved ones! Help us continue the fight by supporting Mike's Mates in any way you can!
Whether you walk with us in person or virtually, donate or ask for donations, every little bit of support makes a difference. Ultimately, we want to spread awareness, raise money, and give hope to those with ALS and their families.
Because of money raised in the past, gene therapy for ALS is becoming a reality! Check out this news report: https://www.nbcboston.com/news/health/incredible-progress-new-research-reports-possible-gene-therapy-for-als/2156171/?fbclid=IwAR0FIVOyZUdG66SyyqtlLFe9BSSsKNJFWzFVNQ59UM1LJGyuEiIIoW4Sk_g
We thank you in advance for helping our small but mighty team reach our fund raising goal! Together we can make a difference in the lives of those affected by Lou Gehrig’s Disease. Our team is committed to raising money to support people in our community with ALS and spread awareness of the urgency to find treatment and a cure. Please consider joining our team in the Walk to Defeat ALS® or choose a team member from the list and donate to our cause.
Why We Need Your Help
Often referred to as Lou Gehrig's Disease, amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of an ALS patient averages 2 to 5 years from the time of diagnosis.
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no discrimination.
This crippling disease can strike anyone. Presently there is no known cause of the disease yet it still costs loved ones an average of $200,000 a year to provide the care ALS patients need. Help make a difference and donate or join a walk today.
